R Run hard@thehsc Active Member Joined Oct 7, 2021 Messages 344 Gender Male HSC 2022 Sunday at 8:26 AM #1 ^^^^ my teacher said it was - but not too sure about it!!!
Nezuko---- New Member Joined May 18, 2020 Messages 2 Gender Male HSC 2022 Sunday at 9:55 AM #2 I believe, so, substitution reactions with Cl2 or Br2 utilise UV Light, correct me if I'm wrong.
R Run hard@thehsc Active Member Joined Oct 7, 2021 Messages 344 Gender Male HSC 2022 Sunday at 10:06 AM #3 yeah they do - its because the reaction requires energy to overcome the Cl2 and Br2 bonds
someth1ng Retired Nov '14 Joined Sep 18, 2010 Messages 5,530 Location Adelaide, Australia Gender Male HSC 2012 Uni Grad 2021 Yesterday at 11:41 AM #4 I'd argue that it's technically wrong to say UV catalysed because the UV is consumed in the reaction. It's more accurate to describe it as UV activated/mediated. Last edited: Today at 2:13 AM
I'd argue that it's technically wrong to say UV catalysed because the UV is consumed in the reaction. It's more accurate to describe it as UV activated/mediated.
R Run hard@thehsc Active Member Joined Oct 7, 2021 Messages 344 Gender Male HSC 2022 Yesterday at 2:17 PM #5 @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst
@someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst
E ekjchale#1 Member Joined Apr 4, 2022 Messages 55 Gender Male HSC 2022 Yesterday at 3:33 PM #6 Run hard@thehsc said: @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst Click to expand... Damn our teachers r similar then lol
Run hard@thehsc said: @someth1ng yh I would agree with that - its just that my teacher confused everyone by saying its a catalyst Click to expand... Damn our teachers r similar then lol